@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_head {
  this: np:hasAssertion dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_assertion;
    np:hasProvenance dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_provenance;
    np:hasPublicationInfo dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_assertion a np:Assertion .
  
  dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_provenance a np:Provenance .
  
  dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_assertion {
  miriam-gene:391723 a ncit:C16612 .
  
  lld:C0238288 a ncit:C7057 .
  
  dgn-gda:DGN765363db91c309e3e2d1ebd1f1aecc3f sio:SIO_000628 miriam-gene:391723, lld:C0238288;
    a sio:SIO_001121 .
}

dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_provenance {
  dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_assertion dcterms:description
      "[A total of 16 genes in the FSHD region (FRG2, TUBB4Q, FRG1, FAT1, F11, KLKB1, CYP4V2, TLR3, SORBS2, PDLIM3 (ALP), LRP2BP, ING2, SNX25, SLC25A4 (ANT1), HELT and IRF2) were examined for interallelic variation in RNA expression within individual myonuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:19888305;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP715055.RAOjF_qjdbxDev1Y7zzEYUeofupW--2d7Zpd2OC5xTSBQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:14+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}